Boron-Templated Dimerization of Allylic Alcohols To Form Protected 1,3-Diols via Acid Catalysis.
暂无分享,去创建一个
Stacey J. Smith | Gabriel A. Valdivia-Berroeta | D. Michaelis | Karissa C. Kenney | S. H. Nazari | Erin E. Martinez | Kyle J. Gassaway | Kelton G Forson | Nicholas J Hansen | Nathan M Lyons | Nathan Lyons | Kelton G. Forson | Nicholas J. Hansen
[1] R. Luque,et al. Functional metal–organic frameworks for catalytic applications , 2019, Coordination Chemistry Reviews.
[2] A. Slawin,et al. Aryl Boronic Acid Catalysed Dehydrative Substitution of Benzylic Alcohols for C-O Bond Formation. , 2019, Chemistry.
[3] K. Raymond,et al. Supramolecular Host-Selective Activation of Iodoarenes by Encapsulated Organometallics. , 2019, Journal of the American Chemical Society.
[4] K. Raymond,et al. Self-Assembled Tetrahedral Hosts as Supramolecular Catalysts. , 2018, Accounts of chemical research.
[5] Norma Tiempos-Flores,et al. C-N Bond Formation from Allylic Alcohols via Cooperative Nickel and Titanium Catalysis. , 2018, The Journal of organic chemistry.
[6] S. Chiu,et al. Using Alkali Metal Ions To Template the Synthesis of Interlocked Molecules. , 2018, Accounts of chemical research.
[7] Rui Zhang,et al. Metal–organic framework-derived porous materials for catalysis , 2018 .
[8] K. Houk,et al. Quinine-Promoted, Enantioselective Boron-Tethered Diels-Alder Reaction by Anomeric Control of Transition-State Conformation. , 2018, Journal of Organic Chemistry.
[9] Suzanne M. Batiste,et al. Evidence for Ion-Templation During Macrocyclooligomerization of Depsipeptides. , 2018, Journal of the American Chemical Society.
[10] Stacey J. Smith,et al. Nickel-Catalyzed Suzuki Cross Couplings with Unprotected Allylic Alcohols Enabled by Bidentate N-Heterocyclic Carbene (NHC)/Phosphine Ligands , 2018 .
[11] Gabriel A. Valdivia-Berroeta,et al. Proximity-Induced Reactivity and Product Selectivity with a Rationally Designed Bifunctional Peptide Catalyst , 2017 .
[12] K. Miyamoto,et al. Transition Metal-Free trans-Selective Alkynylboration of Alkynes. , 2017, Journal of the American Chemical Society.
[13] Rui‐Biao Lin,et al. Coordination templated [2+2+2] cyclotrimerization in a porous coordination framework , 2015, Nature Communications.
[14] S. Luis,et al. Macrocyclization Reactions: The Importance of Conformational, Configurational, and Template-Induced Preorganization. , 2015, Chemical reviews.
[15] M. Rezaeivala,et al. Schiff base and non-Schiff base macrocyclic ligands and complexes incorporating the pyridine moiety – The first 50 years , 2014 .
[16] P. Beer,et al. Advances in anion supramolecular chemistry: from recognition to chemical applications. , 2014, Angewandte Chemie.
[17] Alen Čusak. Temporary silicon-tethered ring-closing metathesis: recent advances in methodology development and natural product synthesis. , 2012, Chemistry.
[18] K. Tan. Induced Intramolecularity: An Effective Strategy in Catalysis , 2011 .
[19] Z. Xi,et al. Zirconocene and Si-tethered diynes: a happy match directed toward organometallic chemistry and organic synthesis. , 2011, Accounts of chemical research.
[20] M. Suginome,et al. Palladium-catalyzed, stereoselective, cyclizative alkenylboration of carbon-carbon double bonds through activation of a boron-chlorine bond. , 2011, Journal of the American Chemical Society.
[21] E. Anderson,et al. Recent advances in the use of temporary silicon tethers in metal-mediated reactions. , 2010, Chemical Society reviews.
[22] H. G. Peer. The reaction of phenol with formaldehyde. III. selective hydroxymethylation of phenols at the ortho‐position , 2010 .
[23] D. Hall,et al. Zirconium-catalyzed Nagata reaction for the synthesis of 2-aryl-1,3,2-aryldioxaborins via a mild three-component condensation of phenols, aldehydes, and boronic acid , 2010 .
[24] M. Suginome,et al. Palladium-catalyzed trans- and cis-carboboration of alkynes tethered to chloroborane with organozirconium reagents: ligand-dependent complementary stereoselectivity. , 2008, Journal of the American Chemical Society.
[25] B. Gibb,et al. Macrocycle Synthesis Through Templation , 2006 .
[26] K. K. Hii,et al. Copper-catalyzed intermolecular hydroamination of alkenes. , 2006, Organic letters.
[27] Kenji Itoh,et al. Cp(*)RuCl-catalyzed formal intermolecular cyclotrimerization of three unsymmetrical alkynes through a boron temporary tether: regioselective four-component coupling synthesis of phthalides. , 2005, Journal of the American Chemical Society.
[28] Yoshihiko Yamamoto,et al. Ru(II)-catalyzed chemo- and regioselective cyclotrimerization of three unsymmetrical alkynes through boron temporary tether. One-pot four-component coupling via cyclotrimerization/Suzuki-Miyaura coupling. , 2004, Journal of the American Chemical Society.
[29] R. Batey,et al. Alkenylboronate Tethered Intramolecular Diels−Alder Reactions , 1999 .
[30] R. Batey,et al. Diels–Alder reactions of dienylboron compounds with unactivated dienophiles: an application of boron tethering for substituted cyclohexenol synthesis , 1999 .
[31] S. Sieburth,et al. Intramolecular Reactions of Temporarily Silicon-Tethered Molecules , 1997 .
[32] K. Nicolaou,et al. Synthesis of a fully functionalized CD ring system of taxol , 1992 .
[33] N. Iwasawa,et al. Phenylboronic Acid as a Template in the Diels-Alder Reaction , 1991 .
[34] W. Nagata,et al. ortho-Specific α-Hydroxyalkylation of Phenols with Aldehydes. An Efficient Synthesis of Saligenol Derivatives , 1979 .